کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
236988 | 465690 | 2012 | 7 صفحه PDF | دانلود رایگان |

This article presents a facile approach about the designed synthesis of one-dimensional (1D) dysprosium-based coordination polymer wires under solvothermal conditions with dysprosium chloride and tributyl phosphate (TBP) as starting materials. The wires are in the length of several hundreds of micrometers and diameter in the range of 0.4–2 μm. Time-dependent results revealed that the coordination polymer wires were not stable and evolved into three-dimensional (3D) flower-like tetragonal DyPO4 superstructures with the prolonging of reaction time. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), selected area electron diffraction (SAED), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), energy disperse spectroscopy (EDS), thermogravimetric analysis (TG) and differential thermal analysis (DTA) were employed to characterize the samples. Interestingly, with the assistance of lauryl sodium sulfate, rice-like macroporous hexagonal DyPO4 microstructures with a BET surface area of 2.13 m2/g were successfully fabricated. A possible formation mechanism for the morphology evolution of the DyPO4 superstructures was also discussed. Magnetic measurement revealed that the products were antiferromagnetic.
Dysprosium-based coordination polymer fibers were prepared via a facile solvothermal method and they evolved to 3D flower-like tetragonal DyPO4 superstructures with the prolonging of solvothermal time. Rice-like macroporous hexagonal DyPO4 nanostructures were obtained with the assistance of lauryl sodium sulfate.Figure optionsDownload as PowerPoint slideHighlights
► One-dimensional (1D) dysprosium-based coordination polymer wires have been prepared.
► 3D flower-like tetragonal DyPO4 nanostructures were prepared.
► Rice-like macroporous hexagonal DyPO4 microstructures were fabricated.
Journal: Powder Technology - Volume 230, November 2012, Pages 151–157